4 Einträge gefunden

1. Edgetic Perturbations Contribute to Phenotypic Variability in PEX26 Deficiency

   1. Lotz-Havla, Amelie S
   2. Woidy, Mathias
   3. Guder, Philipp
   4. Schmiesing, Jessica
   5. Erdmann, Ralf
   6. Waterham, Hans R
   7. Muntau, Ania C

   2021 - Forschungsinformationssystem des UKE - frei zugänglich
2. Inborn errors of metabolism and the human interactome: a systems medicine approach

   1. Woidy, Mathias
   2. Muntau, Ania C
   3. Gersting, Søren W

   2018 - Forschungsinformationssystem des UKE
3. Secondary BH4 deficiency links protein homeostasis to regulation of phenylalanine metabolism

   1. Eichinger, Anna
   2. Danecka, Marta K
   3. Möglich, Tamara
   4. Borsch, Julia
   5. Woidy, Mathias
   6. Büttner, Lars
   7. Muntau, Ania C

   2018 - Forschungsinformationssystem des UKE
4. Mapping the functional landscape of frequent phenylalanine hydroxylase (PAH) genotypes promotes personalised medicine in phenylketonuria

   1. Danecka, Marta K
   2. Woidy, Mathias
   3. Zschocke, Johannes
   4. Feillet, François
   5. Muntau, Ania C
   6. Gersting, Søren W

   2015 - Forschungsinformationssystem des UKE